User's Guide

16 KANSO
®
2 SOUND PROCESSOR USER GUIDE
Certification and applied standards
The Kanso 2 Sound Processor fulfils the essential requirements
listed in Annex 1 of the EC directive 90/385/EEC on Active
Implantable Medical Devices as per the conformity
assessment procedure in Annex 2.

The year in which authorisation to affix the CE mark was
granted was 2020.
It also fulfils the essential requirements of Directive 2014/53/
EU on Radio Equipment as per the conformity assessment
procedure in Annex II. The declaration of conformity may be
consulted at www.cochlear.com/wps/wcm/connect/intl/
about/company-information/declaration-of-conformity
FCC (Federal Communications Commission)
compliance
Changes or modifications not expressly approved by the party
responsible for compliance could void the user’s authority to
operate the equipment.
This device complies with part 15 of the FCC Rules. Operation
is subject to the following two conditions:
1. This device may not cause harmful interference, and
2. This device must accept any interference received,
including interference that may cause undesired operation.
RF exposure safety
This device complies with the FCC RF exposure limits and has
been evaluated in compliance with portable exposure
condition.
There is no limitation as to which distance can be used from
the human body.
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